Cognitive Consequences of High Aβ Amyloid in Mild Cognitive Impairment and Healthy Older Adults: Implications for Early Detection of Alzheimer's Disease

被引:28
作者
Lim, Yen Ying [1 ,2 ]
Ellis, Kathryn A. [1 ,3 ,4 ]
Harrington, Karra [1 ]
Kamer, Adrian [1 ]
Pietrzak, Robert H. [5 ]
Bush, Ashley I. [1 ]
Darby, David [1 ]
Martins, Ralph N. [6 ]
Masters, Colin L. [1 ]
Rowe, Christopher C. [7 ,8 ,9 ]
Savage, Greg [10 ,11 ]
Szoeke, Cassandra [1 ,4 ,12 ]
Villemagne, Victor L. [1 ,7 ,8 ,13 ]
Ames, David [3 ,4 ]
Maruff, Paul [1 ,14 ]
机构
[1] Univ Melbourne, Mental Hlth Res Inst, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Psychiat, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Acad Unit Psychiat Old Age, Dept Psychiat, St Georges Hosp, Kew, Vic, Australia
[4] Natl Ageing Res Inst, Parkville, Vic, Australia
[5] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06520 USA
[6] Edith Cowan Univ, Ctr Excellence Alzheimers Dis Res & Care, Sch Exercise Biomed & Hlth Sci, Perth, WA, Australia
[7] Austin Hlth, Dept Nucl Med, Heidelberg, Vic, Australia
[8] Austin Hlth, Ctr PET, Heidelberg, Vic, Australia
[9] Univ Melbourne, Heidelberg, Vic, Australia
[10] Macquarie Univ, Dept Psychol, Sydney, NSW 2109, Australia
[11] Macquarie Univ, ARC Ctr Excellence Cognit & Its Disorders, Sydney, NSW 2109, Australia
[12] CSIRO Preventat Hlth Flagship, Parkville, Vic, Australia
[13] Univ Melbourne, Austin Hlth, Dept Med, Heidelberg, Vic, Australia
[14] CogState Ltd, Melbourne, Vic, Australia
关键词
A beta amyloid; mild cognitive impairment; healthy controls; cognition; POSITRON-EMISSION-TOMOGRAPHY; FLORBETAPIR F 18; EPISODIC MEMORY; NONDEMENTED INDIVIDUALS; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; DECLINE; BIOMARKERS; POPULATION;
D O I
10.1037/a0032321
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
`Background: It has been proposed that only mild cognitive impairment (MCI) with high A beta amyloid is indicative of incipient Alzheimer's disease (AD), yet MCI with low A beta amyloid may reflect other neurode-generative processes. We aimed to determine the extent to which high A beta amyloid influenced cognitive function in healthy older adults and adults with MCI. Method: Healthy controls ( HC; n = 178) and adults with MCI ( n = 56) enrolled in the Australian Imaging, Biomarkers, and Lifestyle study, underwent positron emission tomography neuroimaging for A beta amyloid and completed an extensive neuropsychological battery, assessing the cognitive domains of verbal and visual episodic memory, executive function, visuoconstruction, attention and processing speed, and language at baseline. Results: MCI with low A beta performed worse than MCI with high A beta on measures of executive function, attention, visuoconstruction and language. No differences were observed between HC high and low A beta groups. When compared with HC with low A beta, both MCI high and low A beta groups performed worse on measures of episodic memory. However, only the MCI low A beta group performed worse than HC low A beta on measures of executive function, attention, visuoconstruction, and language. Conclusions: When compared with HC with low A beta amyloid, MCI with high A beta amyloid present with impairments restricted to episodic memory, and the episodic memory impairments in MCI with low A beta amyloid were accompanied by impairments in executive function, attention, visuoconstruction, and language, suggesting that MCI with high A beta amyloid reflects prodromal AD, although further longitudinal data is required to confirm this.
引用
收藏
页码:322 / 332
页数:11
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